Biotech, Food & Drug

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In today’s hyper-aware environment, concerns about food and drug safety are paramount for both companies and consumers.  The Food and Drug Administration (FDA) and the US Department of Agriculture (USDA) regulates the areas of biotech, food, and drug law. Additionally, laws including the 21st Century Cures Act, and cGMP (Current Good Manufacturing Processes), regulate industry standards/norms in food, cosmetics, and other industry-sectors. Visitors to the National Law Review will find the latest analysis of news, legislation, and upcoming cases/litigation as it relates to this area of law.

With researchers searching for new energy solutions and other developments in biotech, visitors to the NLR will have the opportunity to read content surrounding biosimilars, natural fuel production, medical devices, biotechnology, nanotechnology and materials, and the pharmaceuticals industry. Additionally, content relating to food and drug laws, limits on chemical use in cosmetic products, and other general health/safety topics are covered by the National Law Review and are updated regularly. Additionally, food safety and imports to the United States are also discussed as they become relevant. 

In addition to general health, science, and food/drug, the industry is also closely related to many of the issues related to intellectual property law. New applications for patents, intellectual property, licensing laws, and other areas which are governed by the PTAB court, often crossover into the industry.

New developments in legislation, including the legalization of recreational marijuana has created a new area ripe for legal analysis.  Regulations on how recreational marijuana can be advertised and marketed, distributed and the kind of insurance coverage necessary for dispensaries.  Additionally, employer drug-testing and marijuana statutes have been a hot area of litigation covered by the National Law Review.  

General practices in marketing standards, compliance of federal and state laws/legislation, licensing collaborations, and news related to bringing new products to the market, in the US and abroad, are among the areas visitors to NLR will read about daily. Drug pricing, changes in production standards, regulatory compliance, food safety and handling, drug laws (legalization of marijuana, both recreational and medicinal in the workplace), and labeling and nutritional requirements, are among the many topics covered by the National Law Review daily.

Visitors will always find the latest, up-to-date, most comprehensive coverage on the site. And, news and stories which affect the US, companies which are regulated in the industry, and multinational/international companies, are detailed regularly for NLR readers.

National Law Review Cannabis TwitterFor hourly updates on the latest news about biotech, food & drug, and cannabis laws, regulations, and legislation, be sure to follow our Cannabis X (formerly Twitter) feed, and sign up for complimentary e-news bulletins.

Recent Biotechnology, Food & Drug Administration FDA News

Title
Publication Date Organization Sort descending
May
9
2019
California’s Proposition 65 Website Posts Styrene Fact Sheet Keller and Heckman LLP
Jul
27
2022
New Draft Guidance on Remote Regulatory Assessments Keller and Heckman LLP
May
21
2019
EC Publishes Recommendation on Coordinated Control Plan for Certain Substances Migrating from FCMs Keller and Heckman LLP
Aug
17
2022
Whole Foods Rice Pilaf Slack Fill Lawsuit Dismissed Keller and Heckman LLP
Aug
23
2022
New Study on Heavy Metal Levels in Baby Foods Keller and Heckman LLP
Jun
6
2019
OEHHA Confirms Final Carcinogen/Coffee Rule on Twitter Keller and Heckman LLP
Jun
11
2019
Deadlines Set for FDA to Establish Reporting Requirements for “High-Risk” Foods Keller and Heckman LLP
Jul
18
2019
FDA Proposes Exempting Type III DMFs from Electronic Formatting Requirement Keller and Heckman LLP
Oct
25
2022
FSIS Announces Proposed Framework to Reduce Salmonella Illness from Poultry Keller and Heckman LLP
Jul
24
2019
FDA Announces FSMA Third-Party Certification Program User Fee Rates for Fiscal Year 2020 Keller and Heckman LLP
Oct
31
2022
Nutrition Company’s “Milk-Based” Formula False Advertising Suit Dismissed Keller and Heckman LLP
Nov
8
2022
Pair of Lawsuits Target Mint Flavored Products Keller and Heckman LLP
Aug
1
2019
Flies Are a Potential E. Coli Vector in Leafy Green Illness Outbreaks Keller and Heckman LLP
Nov
29
2022
Singapore Updates Guidelines for the Safety Assessment of Novel Foods Keller and Heckman LLP
Aug
16
2019
FDA Proposes New Graphic Warnings for Cigarettes Keller and Heckman LLP
Dec
5
2022
TTB Plans to Issue New Rules for Alcohol Beverage Labels Keller and Heckman LLP
Dec
13
2022
FDA Letter States that β-Nicotinamide Mononucleotide is Not Lawful Dietary Supplement Keller and Heckman LLP
Aug
23
2019
Update on the Regulation of CBD-Infused Products Keller and Heckman LLP
Jan
9
2023
FDA Removes L. monocytogenes From Protocol for the Development and EPA Registration of Treatments for Preharvest Agricultural Water Keller and Heckman LLP
Jan
20
2023
USDA Expands Generic Label Approval for Meat, Poultry, and Egg Products Keller and Heckman LLP
Oct
9
2019
FDA’s Approach to New Packaging Factor Database Explained at KH Seminar Keller and Heckman LLP
Mar
15
2023
Chocolate Manufacturer Responds to Consumer Class Action for Heavy Metals Keller and Heckman LLP
Oct
2
2015
China's NHFPC Releases Key Food Packaging Standards Keller and Heckman LLP
Nov
11
2015
FDA Seeks Comments on the Meaning of "Natural" Keller and Heckman LLP
Nov
25
2015
Canada Sets Deadline for Electronic Filing-Only of DMFS Keller and Heckman LLP
Nov
19
2019
Who Is Responsible for Compliance Testing? Keller and Heckman LLP
Apr
18
2023
CSPI Petitions FDA to Take Action to Reduce Sodium in Food Keller and Heckman LLP
Nov
25
2019
California Considering Further Restrictions on VOCs in Consumer Products Keller and Heckman LLP
 

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